Cargando…
N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis
This article describes the application of N‐heterocyclic iod(az)olium salts (NHISs) as highly reactive organocatalysts. A variety of mono‐ and dicationic NHISs are described and utilized as potent XB‐donors in halogen‐bond catalysis. They were benchmarked in seven diverse test reactions in which the...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519039/ https://www.ncbi.nlm.nih.gov/pubmed/34160859 http://dx.doi.org/10.1002/chem.202101961 |
_version_ | 1784584365872775168 |
---|---|
author | Boelke, Andreas Kuczmera, Thomas J. Lork, Enno Nachtsheim, Boris J. |
author_facet | Boelke, Andreas Kuczmera, Thomas J. Lork, Enno Nachtsheim, Boris J. |
author_sort | Boelke, Andreas |
collection | PubMed |
description | This article describes the application of N‐heterocyclic iod(az)olium salts (NHISs) as highly reactive organocatalysts. A variety of mono‐ and dicationic NHISs are described and utilized as potent XB‐donors in halogen‐bond catalysis. They were benchmarked in seven diverse test reactions in which the activation of carbon‐ and metal‐chloride bonds as well as carbonyl and nitro groups was achieved. N‐methylated dicationic NHISs rendered the highest reactivity in all investigated catalytic applications with reactivities even higher than all previously described monodentate XB‐donors based on iodine(I) and (III) and the strong Lewis acid BF(3). |
format | Online Article Text |
id | pubmed-8519039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85190392021-10-21 N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis Boelke, Andreas Kuczmera, Thomas J. Lork, Enno Nachtsheim, Boris J. Chemistry Communications This article describes the application of N‐heterocyclic iod(az)olium salts (NHISs) as highly reactive organocatalysts. A variety of mono‐ and dicationic NHISs are described and utilized as potent XB‐donors in halogen‐bond catalysis. They were benchmarked in seven diverse test reactions in which the activation of carbon‐ and metal‐chloride bonds as well as carbonyl and nitro groups was achieved. N‐methylated dicationic NHISs rendered the highest reactivity in all investigated catalytic applications with reactivities even higher than all previously described monodentate XB‐donors based on iodine(I) and (III) and the strong Lewis acid BF(3). John Wiley and Sons Inc. 2021-08-05 2021-09-15 /pmc/articles/PMC8519039/ /pubmed/34160859 http://dx.doi.org/10.1002/chem.202101961 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Boelke, Andreas Kuczmera, Thomas J. Lork, Enno Nachtsheim, Boris J. N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis |
title | N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis |
title_full | N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis |
title_fullStr | N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis |
title_full_unstemmed | N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis |
title_short | N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis |
title_sort | n‐heterocyclic iod(az)olium salts – potent halogen‐bond donors in organocatalysis |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519039/ https://www.ncbi.nlm.nih.gov/pubmed/34160859 http://dx.doi.org/10.1002/chem.202101961 |
work_keys_str_mv | AT boelkeandreas nheterocycliciodazoliumsaltspotenthalogenbonddonorsinorganocatalysis AT kuczmerathomasj nheterocycliciodazoliumsaltspotenthalogenbonddonorsinorganocatalysis AT lorkenno nheterocycliciodazoliumsaltspotenthalogenbonddonorsinorganocatalysis AT nachtsheimborisj nheterocycliciodazoliumsaltspotenthalogenbonddonorsinorganocatalysis |